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FDA 510(k)

HYDRO-S WOUND GEL

K-Number: K942419 · 1994-08-05

ApplicantHymedix Intl., Inc.
Decision Date1994-08-05
Product CodeMGQ
DecisionSubstantially Equivalent

Device Summary

HYDRO-S WOUND GEL is the device name listed in this FDA 510(k) record. The listed applicant is Hymedix Intl., Inc.. It received FDA 510(k) clearance on 1994-08-05 under 510(k) number K942419. The device is classified under product code MGQ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HYDRO-S WOUND GEL?

HYDRO-S WOUND GEL is a medical device that received FDA 510(k) clearance on 1994-08-05. The listed applicant is Hymedix Intl., Inc.. The 510(k) number is K942419.

When did HYDRO-S WOUND GEL receive FDA 510(k) clearance?

HYDRO-S WOUND GEL received FDA 510(k) clearance on 1994-08-05, under 510(k) number K942419.

Who is the listed applicant for HYDRO-S WOUND GEL?

The FDA 510(k) record lists Hymedix Intl., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HYDRO-S WOUND GEL?

The FDA product code for HYDRO-S WOUND GEL is MGQ.

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Other records listing Hymedix Intl., Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K942815HYDROSKIN WOUND DRESSING

Related Devices (Code: MGQ)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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